Clinical Research Associate – Sponsor Dedicated
IQVIA
Posted: 10/20/2026
Senior Clinical Research Associate – Psychiatry
Worldwide Clinical Trials
Posted: 10/20/2026
Clinical Research Nurse – Home Visits
WEP Clinical
Posted: 10/20/2026Clinical Research Nurse – Home Visits, PRN
WEP Clinical
Posted: 10/20/2026Clinical Research Nurse – Home Visits
WEP Clinical
Posted: 10/20/2026Clinical Research Nurse – Home Visits
WEP Clinical
Posted: 10/20/2026Clinical Research Nurse, Home Visits
WEP Clinical
Posted: 10/20/2026
Associate Principal Scientist, Clinical Research
MSD
Posted: 10/20/2026Google Cloud Platform
Biostatistician II
Thermo Fisher Scientific
Posted: 10/20/2026D
Senior Biostatistician
DefinedTalent
Posted: 10/20/2026
Clinical Research Regulatory Specialist
Alcanza Clinical Research
Posted: 10/20/2026Google Cloud Platform
Senior Clinical Research Associate – CNS, Psychiatry
Worldwide Clinical Trials
Posted: 10/19/2026
Senior Clinical Research Associate
ICON plc
Posted: 10/19/2026
Clinical Research Nurse II
Emory University
Posted: 10/19/2026Clinical Research Nurse II
Emory University
Posted: 10/19/2026
Clinical Research Associate, U.S. Expert Network
Alcedis - a HUMA company
Posted: 10/19/2026Google Cloud Platform
Senior Clinical Trial Manager
Stoke Therapeutics
Posted: 10/19/2026
Senior Clinical Data Manager – Contract
BioCryst Pharmaceuticals, Inc.
Posted: 10/17/2026
Assistant Manager, Clinical Research – Neurology
WashU IT
Posted: 10/17/2026
Research Systems Analyst – Clinical Research Unit
WVU Online
Posted: 10/17/2026Google Cloud Platform
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical research coordination, including site monitoring, regulatory compliance, and project management. Proficient in Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines, with a strong focus on subject recruitment and site financial management.
Highest-signal resume keywords
Clinical Research CoordinationGood Clinical Practice (GCP)International Conference on Harmonization (ICH)Electronic Data CaptureSite Monitoring
About the role
Key responsibilities & impact- Perform site monitoring visits, including selection, initiation, monitoring, and close-out visits
- Work with sites to adapt, drive, and track subject recruitment plans
- Administer protocol and study training to assigned sites
- Establish regular communication with sites to manage project expectations and issues
- Evaluate study-site quality and integrity and escalate quality issues
- Track regulatory submissions and approvals, recruitment and enrollment, CRF completion and submission, and data query generation and resolution
- Support the study start-up phase when needed
- Ensure site documents are filed in the Trial Master File and verify Investigator's Site File maintenance
- Create and maintain site-management documentation, monitoring visit findings, action plans, visit reports, and follow-up letters
- Collaborate with study team members to support project execution
- Support development of project subject recruitment plans on a per-site basis when applicable
- Support site financial management and retrieve invoices according to local requirements when applicable
Requirements
What you’ll need- 2.5 years of clinical research coordination experience at site level
- Nursing or University Degree (US Bachelor Level or equivalent) in one of the life sciences
- Knowledge of electronic data capture preferred
- Equivalent combination of education, training and experience
- Must reside in the same country where the job is located
- Experienced candidates sought near major hub airports in the Southeast, Northeast, Central and West regions
- 65–70% nationwide travel required
- Knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Compliance with applicable regulations and sponsor requirements
Benefits
Comp & perks- Incentive plans, bonuses, and/or other forms of compensation may be offered
- Health and welfare benefits may be offered
- Equal opportunity employer
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Site MonitoringRegulatory SubmissionsData Query GenerationProtocol AdministrationStudy TrainingSite Document ManagementProject ExecutionSubject Recruitment PlansQuality EvaluationTrial Master File Maintenance
Soft Skills
CommunicationCollaborationProblem-SolvingProject Management
Industry Keywords
Clinical ResearchLife SciencesComplianceSite Financial ManagementRecruitment and Enrollment